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#' maskFromBSGenome
#'
#' @description
#' Extracts the merge of all the active masks from a \code{\link{BSgenome}}
#'
#' @note
#' This function is memoised (cached) using the \code{\link{memoise}} package. To empty the cache, use \code{\link{forget}(maskFromBSGenome)}
#'
#' @usage maskFromBSGenome(bsgenome)
# @usage maskFromBSGenome(...)
#'
#' @param bsgenome a \code{\link{BSgenome}} object
#'
#' @return
#' A \code{\link{GRanges}} object with the active mask in the \code{\link{BSgenome}}
#'
#' @seealso \code{\link{getGenomeAndMask}}, \code{\link{characterToBSGenome}}, \code{\link{emptyCacheRegioneR}}
#'
#' @examples
#' g <- characterToBSGenome("hg19")
#'
#' maskFromBSGenome(g)
#'
#' @export maskFromBSGenome
#'
#' @importFrom Biostrings masks collapse
#' @importFrom S4Vectors Rle
maskFromBSGenome <- memoise::memoise(function(bsgenome) {
if(!methods::hasArg(bsgenome)) stop("parameter bsgenome is required")
if(!methods::is(bsgenome, "BSgenome")) stop("bsgenome must be a BSGenome object")
if(!methods::is(bsgenome, "MaskedBSgenome")) {
warning("bsgenome is not a MaskedBSgenome. Returning an empty mask.")
return(GenomicRanges::GRanges())
}
#WARNING: This is ugly. Since I have not found a way to extract the positions
#of the masks from a BSGenome object in a simple way,
# we are doing it by iterating over the chromosomes
#get the chromosome names using the getGenomes function, so we get exactly the same chromosomes
chrs <- as.character(GenomicRanges::seqnames(getGenome(bsgenome)))
chr.masks <- sapply(chrs, function(chr) {
mm <- Biostrings::masks(bsgenome[[chr]])
if(is.null(mm)) {
return(NULL)
} else {
mm <- Biostrings::collapse(mm)[[1]]
return(mm)
}})
if(do.call(all, lapply(chr.masks, is.null))) { #If the mask is null for all chromosomes, rise a warning and return an empty GRanges
warning("No mask is active for this BSgenome. Returning an empty mask.")
return(GenomicRanges::GRanges())
}
chr.masks <- sapply(chrs, function(chr) {
if(is.null(chr.masks[[chr]])) {
return(NULL)
} else {
return(GenomicRanges::GRanges(seqnames=S4Vectors::Rle(rep(chr, length(chr.masks[[chr]]))), ranges=chr.masks[[chr]]))
}
})
#Combine the mask for each chromosome into a single mask
mask <- GenomicRanges::GRanges(seqinfo = seqinfo(bsgenome))
for(chr in chrs) {
if(!is.null(chr.masks[[chr]])) {
suppressWarnings(mask <- c(mask, chr.masks[[chr]]))
}
}
return(mask)
})
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